Canonical Allele Identifier: CA1547390971
Gene: CCNO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233587_55233588delinsAC , CM000667.2:g.55233587_55233588delinsAC GRCh38
NC_000005.9:g.54529415_54529416delinsAC , CM000667.1:g.54529415_54529416delinsAC GRCh37
NC_000005.8:g.54565172_54565173delinsAC NCBI36
NG_034201.1:g.5130_5131delinsGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.5:c.-65_-64delinsGT MANE Select ENSP00000282572.4:n.-65_-64delinsGT
ENST00000282572.4:c.-65_-64delinsGT ENSP00000282572.4:n.-65_-64delinsGT
ENST00000501463.2:c.-65_-64delinsGT ENSP00000422485.1:n.-65_-64delinsGT
NM_021147.4:c.-65_-64delinsGT NP_066970.3:n.-65_-64delinsGT
NR_125346.1:n.130_131delinsGT
NR_125347.1:n.130_131delinsGT
NM_021147.5:c.-65_-64delinsGT MANE Select NP_066970.3:n.-65_-64delinsGT
NR_125346.2:n.21_22delinsGT
NR_125347.2:n.21_22delinsGT